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普通可变免疫缺陷中的调节性淋巴细胞俱乐部成员。

Members of the Regulatory Lymphocyte Club in Common Variable Immunodeficiency.

机构信息

Basic and Clinical Immunology, Change affiliation of Ankmalika Abha Gupta to Division of Basic and Clinical Immunology, Irvine, CA, United States.

出版信息

Front Immunol. 2022 May 20;13:864307. doi: 10.3389/fimmu.2022.864307. eCollection 2022.

Abstract

The role of CD4 T regulatory cells is well established in peripheral tolerance and the pathogenesis of the murine model and human autoimmune diseases. CD4 T regulatory cells (CD4 Tregs) have been investigated in common variable immunodeficiency (CVID). Recently, additional members have been added to the club of regulatory lymphocytes. These include CD8 T regulatory (CD8 Tregs), B regulatory (Bregs), and T follicular helper regulatory (T) cells. There are accumulating data to suggest their roles in both human and experimental models of autoimmune disease. Their phenotypic characterization and mechanisms of immunoregulation are evolving. Patients with CVID may present or are associated with an increased frequency of autoimmunity and autoimmune diseases. In this review, we have primarily focused on the characteristics of CD4 Tregs and new players of the regulatory club and their changes in patients with CVID in relation to autoimmunity and emphasized the complexity of interplay among various regulatory lymphocytes. We suggest future careful investigations of phenotypic and functional regulatory lymphocytes in a large cohort of phenotypic and genotypically defined CVID patients to define their role in the pathogenesis of CVID and autoimmunity associated with CVID.

摘要

CD4 调节性 T 细胞在周围耐受和啮齿动物模型及人类自身免疫性疾病的发病机制中起着重要作用。CD4 调节性 T 细胞(CD4 Tregs)已在常见可变免疫缺陷(CVID)中进行了研究。最近,调节性淋巴细胞的俱乐部中又增加了其他成员。这些包括 CD8 调节性(CD8 Tregs)、B 调节性(Bregs)和滤泡辅助性 T 细胞调节性(T)细胞。有越来越多的数据表明它们在人类和自身免疫性疾病的实验模型中都具有作用。它们的表型特征和免疫调节机制正在不断发展。CVID 患者可能出现或与自身免疫和自身免疫性疾病的频率增加有关。在这篇综述中,我们主要关注 CD4 Tregs 的特征以及调节性俱乐部的新成员,以及它们在与自身免疫相关的 CVID 患者中的变化,并强调了各种调节性淋巴细胞之间相互作用的复杂性。我们建议在大量表型和基因型定义明确的 CVID 患者中,对表型和功能调节性淋巴细胞进行仔细研究,以确定它们在 CVID 发病机制和与 CVID 相关的自身免疫中的作用。

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